DE2354653A1 - NEW ESTERS - Google Patents
NEW ESTERSInfo
- Publication number
- DE2354653A1 DE2354653A1 DE19732354653 DE2354653A DE2354653A1 DE 2354653 A1 DE2354653 A1 DE 2354653A1 DE 19732354653 DE19732354653 DE 19732354653 DE 2354653 A DE2354653 A DE 2354653A DE 2354653 A1 DE2354653 A1 DE 2354653A1
- Authority
- DE
- Germany
- Prior art keywords
- ethyl
- propyl
- methyl
- chloroallyl
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 150000001875 compounds Chemical class 0.000 claims description 26
- 239000000460 chlorine Substances 0.000 claims description 22
- -1 propargyloxy Chemical group 0.000 claims description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 19
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 10
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 4
- 239000000969 carrier Substances 0.000 claims description 4
- 241000238631 Hexapoda Species 0.000 claims description 3
- 241000607479 Yersinia pestis Species 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 125000005336 allyloxy group Chemical group 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 241001465754 Metazoa Species 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 235000013311 vegetables Nutrition 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims 12
- 239000010452 phosphate Substances 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 150000002431 hydrogen Chemical class 0.000 claims 4
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical group CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 claims 2
- 125000005210 alkyl ammonium group Chemical group 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 21
- 230000000694 effects Effects 0.000 description 13
- 238000012360 testing method Methods 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 239000008187 granular material Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000005995 Aluminium silicate Substances 0.000 description 5
- 235000012211 aluminium silicate Nutrition 0.000 description 5
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
- 241000238876 Acari Species 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 235000013601 eggs Nutrition 0.000 description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 241000426497 Chilo suppressalis Species 0.000 description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 241001454295 Tetranychidae Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000895 acaricidal effect Effects 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 235000019993 champagne Nutrition 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- 241001124076 Aphididae Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 241000256244 Heliothis virescens Species 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 241000949016 Rhipicephalus bursa Species 0.000 description 2
- 241000238680 Rhipicephalus microplus Species 0.000 description 2
- 241000256250 Spodoptera littoralis Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241001454293 Tetranychus urticae Species 0.000 description 2
- 240000006677 Vicia faba Species 0.000 description 2
- 235000010749 Vicia faba Nutrition 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000003032 phytopathogenic effect Effects 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical class OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 1
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 1
- 241000254032 Acrididae Species 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000238888 Argasidae Species 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241000238660 Blattidae Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000257161 Calliphoridae Species 0.000 description 1
- 241001414835 Cimicidae Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000256113 Culicidae Species 0.000 description 1
- 241000131287 Dermestidae Species 0.000 description 1
- 235000009161 Espostoa lanata Nutrition 0.000 description 1
- 240000001624 Espostoa lanata Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
- 241000238816 Gryllidae Species 0.000 description 1
- 241001243087 Gryllotalpidae Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 241000238889 Ixodidae Species 0.000 description 1
- 241001124557 Lymantriidae Species 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- 241000256259 Noctuidae Species 0.000 description 1
- 241000233654 Oomycetes Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000255893 Pyralidae Species 0.000 description 1
- 241001124072 Reduviidae Species 0.000 description 1
- 241000254062 Scarabaeidae Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 241000254107 Tenebrionidae Species 0.000 description 1
- 241000255588 Tephritidae Species 0.000 description 1
- 241000896028 Tettigoniidae Species 0.000 description 1
- 241000130767 Tineidae Species 0.000 description 1
- 241000131339 Tipulidae Species 0.000 description 1
- 235000002098 Vicia faba var. major Nutrition 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005133 alkynyloxy group Chemical group 0.000 description 1
- DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- 235000005489 dwarf bean Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000199 molecular distillation Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003555 thioacetals Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/18—Esters of thiophosphoric acids with hydroxyaryl compounds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Dr. F. ZumstQin ssn. - Dr. E. Assmann Dr.R.Koöriiy3l«cr.-;cr - Dr1:1. PUys.R. HolzbauerDr. F. ZumstQin ssn. - Dr. E. Assmann Dr.R.Koöriiy3l «cr .-; cr - Dr 1 : 1. PUys.R. Timber builder
E>r. F. 2u in rl; in jun,E> r. F. 2u in rl; in jun,
PatentanwältePatent attorneys
8. fA 0 η c h e π 2, Bräuhausjtraßo 4 / III8. fA 0 η che π 2, Bräuhausjtraßo 4 / III
Case 5-8499/l+2/? _
Deutschland Case 5-8499 / l + 2 / ? _
Germany
Neue EsterNew esters
Die vorliegende Erfindung betrifft Thio- resp. Dithiophosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung. Die Thio- resp. Dithiophosphorsäureester haben dieThe present invention relates to thio respectively. Dithiophosphoric acid ester, Process for their production and their use in pest control. The thio resp. Dithiophosphoric acid esters have the
Formelformula
/-— 5K ^ / - 5 K ^
. (D. (D
A09820/.1209A09820 / .1209
worin Rwhere R
L2 L 2
U und R4 U and R 4
Methyl oder Aethyl, n-Propyl, Isobutyl oder sek.-Butyl, Chlor, Brom, Methyl oder Aethyl, -OCOCH3, -O-C3-C5-Alkenyl, -0-C3-C5-Alkinyl, -0-C1-C,-Alkylen-0-C1-C4-Alkyl, -0"C -0-CH2-CH=CHCI, -SCH2 -S-C-j-Cc-Alkenyl, SCN, -CH2CH=CHCl, -CHO, -Methyl or ethyl, n-propyl, isobutyl or sec-butyl, chlorine, bromine, methyl or ethyl, -OCOCH 3 , -OC 3 -C 5 -alkenyl, -0-C 3 -C 5 -alkynyl, -0- C 1 -C, -alkylene-0-C 1 -C 4 -alkyl, -0 "C- O-CH 2 -CH = CHCl, -SCH 2 -SCj-Cc -alkenyl, SCN, -CH 2 CH = CHCl , -CHO, -
-CH.-CH.
"O-"O-
CH,CH,
-CH.-CH.
-CH-CH
O-rCH.O-rCH.
o-Jo-y
-CH--CH-
0—fCH0 — fCH
-CH-CH
-CH,-CH,
-CH-CH
OC1-C4-AlkylOC 1 -C 4 alkyl
OC1-C4-AIlCyI CH OC 1 -C 4 -AlCyI CH
SC1 -C,-AlkylSC 1 -C, -alkyl
S—1S — 1
-CH -CH.-CH -CH.
S—rCHS — rCH
-CH-CH
, -ch;, -ch;
:γ: γ
409820/1209409820/1209
23548532354853
, -CH=N-C1-C4-Alkyl, CH=N-NH-C1-C4-Alkyl oder, -CH = NC 1 -C 4 -alkyl, CH = N-NH-C 1 -C 4 -alkyl or
, C1-C4-AIk7I, C 1 -C 4 alk 7 I.
CH=N-N undCH = N-N and
X Sauerstoff oder Schwefel bedeuten.X represent oxygen or sulfur.
Die bei R1- in Frage kommenden Alkenyloxy-, Alkinyloxy-, Alkoxyalkylenoxy- oder Alkenylthibgruppen können geradkettig oder verzweigt sein. Beispiele solcher Gruppen sind u.a.: Allyloxy, Methallyloxy, Propargyloxy, l-Methyl-2-propinyloxy, l,l-Dimethyl-2-propinyloxys (l-Methyl-2-methoxy)-äthoxy, 2-Methoxy-athoxy, 2-Aethoxy=- ^'äthoxy, Allylthio, Methallylthio.The alkenyloxy, alkynyloxy, alkoxyalkyleneoxy or alkenylthib groups which come into question for R 1 - can be straight-chain or branched. Examples of such groups include: allyloxy, methallyloxy, propargyloxy, l-methyl-2-propinyloxy, l, l-dimethyl-2-propinyloxy s (l-methyl-2-methoxy) ethoxy, 2-methoxy-ethoxy, 2- Ethoxy = - ^ 'ethoxy, allylthio, methallylthio.
Die Alkyl-Teile einer Acetal-, Thioacetal-, n-Alkylformimino-, N-Alkylhydrazono- oder N,N-Dialkylhydrazonogruppe R,-sind geradkettig, Beispiele solcher Teil-Gruppen sind u.a.: Methyl, Aethyl.The alkyl parts of an acetal, thioacetal, n-alkylformimino, N-alkylhydrazono or N, N-dialkylhydrazo group R 1 - are straight-chain, examples of such sub-groups include: methyl, ethyl.
409820/1209409820/1209
235A653235A653
Eine bevorzugte Gruppe bilden die Verbindungen der FormelThe compounds of the formula form a preferred group
worin R, Methyl oder Aethyl, R„ n-Propyl oder sek.-Butyl,wherein R, methyl or ethyl, R "n-propyl or sec-butyl,
R. und R/ je Wasserstoff, Chlor, Brom, Methyl oder Aethyl, R5 Allyloxy, Methallyloxy, 2-Chlorallyloxy,R. and R / each hydrogen, chlorine, bromine, methyl or ethyl, R 5 allyloxy, methallyloxy, 2-chloroallyloxy,
"3-Chlorallyloxy, Propargyloxy, Allylthio oder"3-chloroallyloxy, propargyloxy, allylthio or
Methällylthio und X Sauerstoff bedeuten.Methällylthio and X represent oxygen.
Eine weitere bevorzugte Gruppe bilden die Verbindungen der Formel I,Another preferred group is formed by the compounds of the formula I,
worin R, Methyl oder Aethyl,wherein R, methyl or ethyl,
R2 n-Propyl oder sek.-Butyl, Ro und R, je Wasserstoff, Chlor, Brom, Methyl oderR 2 n-propyl or sec-butyl, Ro and R, each hydrogen, chlorine, bromine, methyl or
Aethyl,,
R5 -CHO, -CH-N-Q» , -CH=N-C3H7(I),Ethyl,,
R 5 -CHO, -CH-NQ », -CH = NC 3 H 7 (I),
-CH=N-N(CH3)2 , -O-CH = NN (CH 3 ) 2 , -O
OCH3 OCH 3
x , CH\ » CH x , CH \ » CH
SCnHr SCnHrSCREW SCREW
£098207120$£ 098 207 120 $
-ο--ο-
-ch:-ch:
ο-ο-
-CH,-CH,
CH,CH,
CH3 CH 3
, -ch;, -ch;
•0-i• 0-i
0-J-CH,0-J-CH,
-CH.-CH.
-ch;-ch;
-CH.-CH.
-CH,-CH,
-CH-CH
S—'S— '
-C2H5 -C 2 H 5
S—ιS-ι
undand
CH,CH,
Sauerstoff bedeuten.Mean oxygen.
Eine weitere bevorzugte Gruppe bilden die Verbindungen der Formel I,Another preferred group is formed by the compounds of the formula I,
worin R-, Methyl oder Aethyl,wherein R-, methyl or ethyl,
R« n-Propyl oder sek.-Butyl, : R 'is n-propyl or sec-butyl:
Ro und R, je Wasserstoff, Chlor, Brom, MethylRo and R, each hydrogen, chlorine, bromine, methyl
oder Aethyl, ;'or ethyl,; '
R5 2-Chlorallyl oder 3-Chlorallyl und ;R 5 is 2-chloroallyl or 3-chloroallyl and;
X Sauerstoff bedeuten.X mean oxygen.
409820/1209409820/1209
Aufgrund ihrer Wirkung besonders hervorzuheben sindParticularly noteworthy because of their effect
; die Verbindungen der Formel I,; the compounds of formula I,
worin R, Aethyl, ■wherein R, ethyl, ■
R2 n-Propyl oder sek.-Butyl, • Ro und R, je Wasserstoff, Chlor, Brom oderR 2 n-propyl or sec-butyl, • Ro and R, each hydrogen, chlorine, bromine or
ι ----■—ι ---- ■ -
Methyl bedeuten und . Rr in ortho-Stellung steht undMean methyl and. Rr is in the ortho position and
2-Chlorallyl oder 3-Chlorallyl bedeutet.2-chloroallyl or 3-chloroallyl means.
Die Verbindungen der Formel I können nach an sich bekannten Methoden z.B. wie folgt hergestellt werden:The compounds of the formula I can be prepared by methods known per se, for example as follows:
säureMndendesx. Mittel ~s acid mouth desx . Means ~ s
R1CK IiR 1 CK Ii
L >P-C1
R2S^ L > P-C1
R 2 S ^
(II)(II)
In den Formeln II, III und IV haben R1 bis R5 und X die für die Formel I angegebene Bedeutung und Me steht für ein Alkalimetall, insbesondere Natrium oder Kalium, Ammonium oder Alkylaramonium. In the formulas II, III and IV, R 1 to R 5 and X have the meaning given for the formula I and Me stands for an alkali metal, in particular sodium or potassium, ammonium or alkyl aramonium.
409820/ 1209409820/1209
Die Verfahren la und Ib können bei normalem Druck, bei einer Temperatur von 0 - 80 PC, vorzugsweise 20 - 500C und in gegenüber den Reaktionsteilnehmern inerten Lösungsund Verdünnungsmitteln durchgeführt werden. Als Lösungs- oder Verdünnungsmittel eignen sich z.B.: Aether und ätherartige Verbindungen, wie Diäthylather, Dipropylather, Dioxan, Tetrahydrofuran; Amide, wie N,N-dialkylierte Carbonsäureamide; aliphatische, aromatische sowie halogenierte Kohlenwasserstoffe, insbesondere Benzol, Toluol, Xylole, Chloroform, Chlorbenzol; Nitrile wie Acetonitril. *The method la and Ib can at normal pressure, at a temperature from 0 to 80 P C, preferably 20 - 50 0 C and are performed in respect to the reactants, solvents and inert diluents. Examples of suitable solvents or diluents are: ethers and ethereal compounds, such as diethyl ether, dipropyl ether, dioxane, tetrahydrofuran; Amides, such as N, N-dialkylated carboxamides; aliphatic, aromatic and halogenated hydrocarbons, in particular benzene, toluene, xylenes, chloroform, chlorobenzene; Nitriles such as acetonitrile. *
Die Ausgangsstoffe der Formel II sind bekannt und können analog z.B, nach der im J. org. Chem, 30 3217 (1965) beschriebenen Methode hergestellt werden. Die Wirkstoffe der Formel I eignen sieh zur Bekämpfung verschiedenartigsten tierischen und pflanzlichen Schädlinge. The starting materials of the formula II are known and can analogously, for example, according to the J. org. Chem, 30, 3217 (1965) Method. The active ingredients of the formula I are suitable for combating various animal and vegetable pests.
Insbesondere zeigen sie eine gute Wirkung gegen alle Entwicklungsstadien, wie Eier, Larven, Nymphen, Puppen und Adulte von Insekten, wie z.B. Insekten der Familien: Acrididae, Blattidae, Gryllidae, Gryllotalpidae, Tettigoniidae, Cimicidae, Phyrrhocoridae, Reduviidae, Aphididae, Delphacidae, piaspididae, Pseudoeoccidae, Chrysomelidaej Coecinellidae, Bruehidae, Scarabaeidae, Dermestidae, Tenebrionidae, Cureulionidae, Tineidae, Noctuidae? In particular, they show a good action against all stages of development, such as eggs, larvae, nymphs, pupae and adults of insects, such as, for example, insects of the families: Acrididae, Blattidae, Gryllidae, Gryllotalpidae, Tettigoniidae, Cimicidae, Phyrrhocoridae, Reduviidae, Aphididae, Delphiasacididae , Pseudoeoccidae, Chrysomelidaej Coecinellidae, Bruehidae, Scarabaeidae, Dermestidae, Tenebrionidae, Cureulionidae, Tineidae, Noctuidae ?
4Q902Q/12Q94Q902Q / 12Q9
Lymantriidae, Pyralidae, Galleriidae, Culicidae, Tipulidae, Stomoxydae, Muscidae, Calliphoridae, Trypetidae, Pulieidae. Lymantriidae, Pyralidae, Galleriidae, Culicidae, Tipulidae, Stomoxydae, Muscidae, Calliphoridae, Trypetidae, Pulieidae.
Die Verbindungen der Formel I wirken auch gegen Eier, Larven und Adulte von Vertretern der Ordnung Akarina. wie Milben, Spinnrailben und Zecken, z.B. der Familien: Ixodidae, Argasidae, Tetranychidae und Demanyssidae. Die insektizide oder akarizide Wirkung lasst sich durch Zusatz von anderen Insektiziden und/oder Akariziden wesentlich verbreitern und an gegebene Umstände anpassen. Als Zusätze eignen sich z.B.:The compounds of formula I are also effective against eggs, Larvae and adults of representatives of the order Akarina. such as mites, spider mites and ticks, e.g. of families: Ixodidae, Argasidae, Tetranychidae and Demanyssidae. The insecticidal or acaricidal effect can be let through Substantially broaden the addition of other insecticides and / or acaricides and adapt to the given circumstances. Suitable additives are, for example:
organische Phosphorverbindungen,organic phosphorus compounds,
Derivate von Nitrophenolen,Derivatives of nitrophenols,
Formamidine,
Harnstoffe,Formamidine,
Ureas,
Carbamate undCarbamates and
chlorierte Kohlenwasserstoffe.chlorinated hydrocarbons.
Die Verbindungen der Formel I weisen neben den oben erwähnten Eigenschaften auch eine Wirksamkeit gegen Fungi auf, z.B. gegen die phytopathogenen Pilze der Klasse: Oomycetes, Zygomycetes, Ascomycetes, Basidiomycetes, Denteromycetes.In addition to the properties mentioned above, the compounds of the formula I also have an activity against fungi e.g. against the phytopathogenic fungi of the class: Oomycetes, Zygomycetes, Ascomycetes, Basidiomycetes, Denteromycetes.
Sie weisen auch eine Wirksamkeit gegen pflanzenpathogene Nematoden auf.They also show activity against phytopathogenic nematodes.
09820/120909820/1209
Die Verbindungen der Formel I können für sich allein oder zusammen mit geeigneten Trägern und/oder Zuschlagstoffen eingesetzt werden. Geeignete Träger und Zuschlagstoffe können fest oder flüssig sein und entsprechen den in der Formulierungstechnik Üblichen Stoffen-wie z.B. naturlichen ' oder regenerierten Stoffen, Lösungs-, Dispergier-, Netz-, Haft-, Verdickungs-, Binde- und/oder Düngemitteln. Zur Applikation können die Verbindungen der Formel I zu Stäubemitteln, Emulsionskonzentraten, Granulaten, Dispersionen, Sprays, zu Lösungen oder Aufschiämmungen in üblicher Formulierung, die in der Applikationstechnik zum Allgemeinwissen gehören,verarbeitet werden. Die Herstellung erfindungsgemässer Mittel erfolgt in an sich bekannter Weise durch inniges Vermischen und/oder Vermählen von Wirkstoffen der Formel I mit den geeigneten Trägerstoffen, gegebenenfalls unter Zusatz von gegenüber den Wirkstoffen inerten Dispergier- oder Lösungsmitteln. Die Wirkstoffe können in den folgenden Aufarbeitungs- . formen vorliegen und angewendet werden:The compounds of formula I can be used alone or together with suitable supports and / or aggregates can be used. Suitable carriers and additives can be solid or liquid and correspond to those in the Formulation technology Usual substances - such as natural ' or regenerated substances, solvents, dispersants, wetting agents, adhesives, thickeners, binders and / or fertilizers. For application, the compounds of the formula I can be added to dusts, emulsion concentrates, granules, dispersions, Sprays, solutions or slurries in common Formulations that are part of general knowledge in application technology can be processed. The compositions according to the invention are produced in a manner known per se by intimate mixing and / or Milling of active ingredients of the formula I with the suitable carriers, optionally with the addition of opposite dispersants or solvents that are inert to the active ingredients. The active ingredients can be used in the following work-up. forms are available and used:
• 40982 0/1209• 40982 0/1209
Aufarbeitungsformen: Stäubemittel, Streumittel,Forms of processing: dust, grit,
Granulate, Umhüllungsgranulate, Imprägnierungsgranulate und HomogengranulateGranulates, coated granulates, Impregnation granules and homogeneous granules
FlUssigeLiquid
Aufarbeitungsformen:Forms of processing:
a) in Wasser dispergierbare
Wirkstoffkonzentrate: Spritzpulver (wettable powders)a) dispersible in water
Active ingredient concentrates: wettable powders
Pasten, Emulsionen;Pastes, emulsions;
b) Lösungenb) Solutions
Der Gehalt an Wirkstoff in den oben beschriebenen Mitteln liegt zwischen 0,1 bis 95%, dabei ist zu erwähnen, dass bei der Applikation aus dem Flugzeug oder mittels anderer geeigneter Applikationsgeräte Konzentrationen bis zu 99,5 % eingesetzt werden können.The content of active ingredient in the means described above is between 0.1 and 95%, it should be mentioned that when applying from an airplane or by means of another suitable application devices, concentrations of up to 99.5% can be used.
409820/1209409820/1209
«K « OrtO«K« OrtO
Die Wirkstoffe der Formel I können beispielsweise wie folgt formuliert werden:The active ingredients of the formula I can, for example, be formulated as follows:
Stäubemittel: Zur Herstellung eines a) 5%igen und b) 2%igen Stäubemittels werden die folgenden Stoffe verwendet : Dust: The following substances are used to produce a) 5% and b) 2% dust:
a) 5 Teile Wirkstoff
95 Teiie Talkum;a) 5 parts of active ingredient
95 parts of talc;
b) 2 Teile Wirkstoffb) 2 parts of active ingredient
1 Teil hochdisperse Kieselsäure, 97 Teile Talkum1 part of highly disperse silica, 97 parts of talc
Die Wirkstoffe werden mit den Trägerstoffen vermischt und vermählen.The active ingredients are mixed with the carriers and marry.
Granulat: Zur Herstellung eines 5%igen Granulates werden die folgenden Stoffe verwendet: Granules: The following substances are used to produce 5% granules:
■5 Teile Wirkstoff . ■■ 5 parts of active ingredient. ■
0,25 Teile Epichlorhydrin, 0,25 Teile Cetylpolyglykoläther, . '0.25 part of epichlorohydrin, 0.25 part of cetyl polyglycol ether,. '
3,50 Teile Polyäthylenglykol 91 Teile Kaolin (Korngrösse 0,3 - 0,8 mm). Die Aktivsubstanz wird mit Epichlorhydrin vermischt und mit 6 Teilen Aceton gelöst, hierauf wird Polyäthylenglykol und Cetylpolyglykoläther zugesetzt. Die so erhaltene Lösung wird auf Kaolin aufgesprüht und anschliessend das3.50 parts of polyethylene glycol 91 parts of kaolin (grain size 0.3-0.8 mm). The active substance is mixed with epichlorohydrin and dissolved with 6 parts of acetone, then polyethylene glycol is added and cetyl polyglycol ether added. The solution obtained in this way is sprayed onto kaolin and then the
09820/120909820/1209
Aceton im Vakuum verdampft.Acetone evaporated in vacuo.
Spritzpulver: Zur Herstellung eines a) 40%igen, b) und c) 25%igen'd) 10%igen Spritzpulvers werden folgende Bestandteile verwendet: Spray powder: The following ingredients are used to produce a) 40%, b) and c) 25% d) 10% spray powder:
a) 40. Teile Wirkstoffa) 40. parts of active ingredient
5 Teile Ligninsulfonsäure-Natriumsalz,5 parts of lignin sulfonic acid sodium salt,
1 Teil Dibutylnaphthalinsulfonsäure-Natriumsalz,1 part dibutylnaphthalenesulfonic acid sodium salt,
54 Teile Kieselsäure;54 parts of silica;
b) 25 Teile Wirkstoffb) 25 parts of active ingredient
4,5 Teile Calcium-Liginsulfonat,4.5 parts calcium ligin sulfonate,
1,9 Teile Champagne-Kreide/Hydroxyäthylcellulose-Gemisch (1:1),1.9 parts of champagne chalk / hydroxyethyl cellulose mixture (1: 1),
1,5 Teile Natrium-dibutyl-naphthalinsulfonat, 19,5 Teile Kieselsäure, 19,5 Teile Champagne-Kreide, 28,1 Teile Kaolin;1.5 parts of sodium dibutyl naphthalene sulfonate, 19.5 parts of silica, 19.5 parts of Champagne chalk, 28.1 parts of kaolin;
c) 25 Teile Wirkstoffc) 25 parts of active ingredient
2,5 Teile Isooe ty !phenoxy -polyoxyäthylen-ä'thanol, 1,7 Teile Champagne-Kreide/Hydroxyäthylcellulose-2.5 parts of Isooe ty! Phenoxy-polyoxyethylene-ethanol, 1.7 parts champagne chalk / hydroxyethyl cellulose
Gemisch (1:1), 8,3 Teile Natriumaluminiumsilikat,Mixture (1: 1), 8.3 parts of sodium aluminum silicate,
16,5 Teile Kieselgur, Teile Kaolin;16.5 parts of kieselguhr, parts of kaolin;
409820/1209409820/1209
d) 10 Teile Wirkstoffd) 10 parts of active ingredient
3 Teile Gemisch der Natriumsalze von gesättigten3 parts mixture of the sodium salts of saturated
Fettalkoholsulfaten, t 5 Teile Napthalinsulfonsäure/Formaldehyd-Kondensat, Fatty alcohol sulfates, t 5 parts naphthalenesulfonic acid / formaldehyde condensate,
82 Teile Kaolin.82 parts of kaolin.
Die Wirkstoffe werden in geeigneten Mischern mit den Zuschlagstoffen innig vermischt und auf entsprechenden Mühlen und Walzen vermählen. Man erhält Spritzpulver, die sich mit Wasser zu Suspensionen jeder gewünschten Konzentration verdünnen lassen.The active ingredients are mixed with the additives in suitable mixers intimately mixed and ground on appropriate mills and rollers. One receives wettable powder that can be diluted with water to form suspensions of any desired concentration.
Emulgierbare Konzentrate: Zur Herstellung eines a) 10%igen und b) 25%igen emulgierbaren Konzentrates werden folgende Stoffe verwendet: . Emulsifiable concentrates: The following substances are used to produce a) 10% and b) 25% emulsifiable concentrate:.
a) IO Teile Wirkstoffa) IO parts active ingredient
3.4 Teile epoxydiertes Pflanzenöl,3.4 parts epoxidized vegetable oil,
13,4 Teile eines Kombinationsemulgators, bestehend aus Fettalkoholpolyglykoläther und Alkylarylsulfonat-Calciutn-Salz, ■13.4 parts of a combination emulsifier, consisting of fatty alcohol polyglycol ether and alkylarylsulfonate calcium salt, ■
40 Teile Dimethylformamid,40 parts of dimethylformamide,
43,2 Teile Xylol;43.2 parts of xylene;
b) 25 Teile Wirkstoffb) 25 parts of active ingredient
2.5 Teile epoxydiertes Pflanzenöl,2.5 parts epoxidized vegetable oil,
•10 Teile eines Alkylarylsulfonat/Fettalkoholpolyglykoläther-Gemisches, • 10 parts of an alkylarylsulfonate / fatty alcohol polyglycol ether mixture,
409820/1209409820/1209
5 Teile Dimethylformamid, 57,5 Teile Xylol. . ·5 parts of dimethylformamide, 57.5 parts of xylene. . ·
Aus solchen Konzentraten können durch Verdünnen mit Wasser Emulsionen jeder gewünschten Konzentration hergestellt werden.Emulsions of any desired concentration can be prepared from such concentrates by dilution with water will.
Sprühmittel: Zur Herstellung eines 5%igen Sprühmittels werden die folgenden Bestandteile verwendet: Spray: The following ingredients are used to produce a 5% spray:
5 Teile Wirkstoff,5 parts active ingredient,
1 Teil Epichlorhydrin, 94 Teile Benzin (Siedegrenzen 160 - 1900C)1 part epichlorohydrin, 94 parts gasoline (boiling point 160 - 190 0 C)
4 0 9 8 2 0/12094 0 9 8 2 0/1209
Herstellung von O-Aethyl-S- (tf);-propyl-0-4-f ormylphenylthiophosphor säureester , Production of O-ethyl-S- (tf); - propyl-0-4-formylphenylthiophosphoric acid ester ,
17 g 4-Hydroxibenzaldehyd werden in 150 ml Benzol gelöst-, dann werden 13,3 g Triäthylamin zugefügt. Bei 10 - 15°C wird unter ständigem Rühren 26,4 g O-Aethyl-S-(h)-propylehlorthiolphosphorsäureester zugetropft.17 g of 4-hydroxibenzaldehyde are dissolved in 150 ml of benzene, then 13.3 g of triethylamine are added. At 10 - 15 ° C is with constant stirring 26.4 g of O-ethyl-S- (h) -propylehlorthiolphosphorsäureester added dropwise.
Nach 12-stUndigem Rühren bei Raumtempratur wird mit Wasser, 3%iger Na2COo-Lösung und wieder mit Wasser gewaschen und über wasserfreiem Natriumsulfat getrocknet. Das Benzol wird abdestilliert. Nach der Molekulardestillation des Rückstandes erhält man die Verbindung der FormelAfter stirring for 12 hours at room temperature, it is washed with water, 3% Na 2 COo solution and again with water and dried over anhydrous sodium sulfate. The benzene is distilled off. After molecular distillation of the residue, the compound of the formula is obtained
CHOCHO
23
mit einer Refraktion von nD ~ 1,5350..23
with a refraction of n D ~ 1.5350 ..
Auf analoge Weise werden auch folgende Verbindungen hergestellt: .The following connections are also established in an analogous manner:.
0
C2H5OvH0
C 2 H 5 OvH
4098207120940982071209
354653354653
Physikalische DatenPhysical data
CHOCHO
OCHOCH
3 ■3 ■
CHOCHO
I=N-H (CH3 )I = NH (CH 3 )
CH=N-N(CHj.CH = N-N (CHj.
I
ClI.
Cl
-CH=N--CH = N-
CHOCHO
-Br-Br
CHOCHO
CHO = 1,540CHO = 1.540
= 1,5460= 1.5460
= 1,5435= 1.5435
= 1,5786= 1.5786
=1,5921= 1.5921
= 1,5320= 1.5320
2020th
11D 11 D
= 1,5293= 1.5293
= 1,5526= 1.5526
= 1,5290= 1.5290
409820/1209409820/1209
75,11.32975.11,329
Physikalische DatenPhysical data
BrBr
-CHO-CHO
COCH,COCH,
1COOH, 1 1 COOH, 1
-S-CH.-NS.
Η,Η,
CHCH
CHCH
CH / \CH / \
CHCH
= 1,5584= 1.5584
χξ3 χξ 3
2222nd
= 1,5152= 1.5152
= 1,5242= 1.5242
2020th
= 1,5762= 1.5762
= 1,5806= 1.5806
22
11D22nd
11 D
= 1,5791= 1.5791
=1,5254= 1.5254
2020th
= 1,5131= 1.5131
4 Q 9 8 2 G / 1 2 0 94 Q 9 8 2 G / 1 2 0 9
/ \CH
/ \
5 X SCH "
5
nD20th
n D
A09820/1209A09820 / 1209
Physikalische DatenPhysical data
-Cl-Cl
CHCH
CHSCHS
CHCH
CHCH
CH / \CH / \
S SS S
'CE,'CE,
CHCH
ΐξ° = 1,5674 ΐξ ° = 1.5674
=.1,5783= .1.5783
= 1,5698= 1.5698
2020th
= 1,5765= 1.5765
= 1,587= 1.587
409820/1209409820/1209
75.tt.32975.tt.329
Physikalische DatenPhysical data
CHCH
~S SC0Hr-2 5~ S SC 0 Hr-2 5
CH2-CH=CH-ClCH 2 -CH = CH-Cl
ι- 5 ι- 5
CH2-CH=CH-ClCH 2 -CH = CH-Cl
•Br '• Br '
CH2-CH=CH-ClCH 2 -CH = CH-Cl
ClCl
CH2-CH=CH-Cl = 1,5705CH 2 -CH = CH-Cl = 1.5705
= 1,5600= 1.5600
= 1,5346= 1.5346
= 1,5318= 1.5318
2020th
= 1,5532= 1.5532
n^ * 1,5400 = 1,5419 n ^ * 1.5400 = 1.5419
409820/1209409820/1209
Physikalische DatenPhysical data
CH2-C=CH2 ClCH 2 -C = CH 2 Cl
S-CH2-C=CH2 3S-CH 2 -C = CH 2 3
I
CH- I.
CH-
0-CH2-CH=CH2 0-CH 2 -CH = CH 2
0-CH2-CH=CH2 0-CH 2 -CH = CH 2
p Oil—p Oil—
OCH2-C=CH = 1,5299OCH 2 -C = CH = 1.5299
= 1,5489= 1.5489
= 1,5542= 1.5542
n^° = 1,5245n ^ ° = 1.5245
=1,5220= 1.5220
20
nD20th
n D
= 1,5225= 1.5225
=1,5308= 1.5308
409.8 2 0/12 09409.8 2 0/12 09
Physikalische DatenPhysical data
OCH2-C=CHOCH 2 -C = CH
I0-C=CHI 0 -C = CH
0-CH2-C=CHO-CH 2 -C = CH
OCH2-CH=CH-ClOCH 2 -CH = CH-Cl
ClCl
Γ
OCH-CH2-OCH Γ
OCH-CH 2 -OCH
ClCl
CHOCHO
,20 , 20
= 1,5290= 1.5290
20
nD20th
n D
= 1,5298= 1.5298
= 1,5219= 1.5219
= 1,5334= 1.5334
= 1,5244= 1.5244
= 1,5102= 1.5102
20
nD20th
n D
= 1,5430= 1.5430
n£u = 1,5372n £ u = 1.5372
409820/1209409820/1209
-- 23 -- 23 -
Physikalische DatenPhysical data
CHCH
3 CHO 3 CHO
CH, 3 CH, 3
■Br CHO ■ Br CHO
ClCl
CHOCHO
. ■ I ·. ■ I ·
-SCN-SCN
SCNSCN
ClCl
CH2-C=CH2 Cl = 1,5530CH 2 -C = CH 2 Cl = 1.5530
= 1,5591= 1.5591
20
nD20th
n D
=1,5418= 1.5418
= 1,5669= 1.5669
2020th
= 1,5565= 1.5565
22
nD22nd
n D
22
nD22nd
n D
1,5489 1,55681.5489 1.5568
2020th
β 1,5272β 1.5272
40982 0/120 9.40982 0/120 9.
CH2-C=CH2
Cl -Cl
CH 2 -C = CH 2
Cl -
n^0 = 1,5355n ^ 0 = 1.5681
n ^ 0 = 1.5355
409820/1209409820/1209
Auf analoge Weise werden noch folgende Verbindungen hergestellt: The following connections are made in the same way:
S .S.
I CH
I.
4 0 9 8 2 0/12094 0 9 8 2 0/1209
R1 Physikalische DatenR 1 physical data
CHCH
c/Vc / V
CH2-CH=CH-GlCH 2 -CH = CH-Eq
-Br-Br
CHOCHO
COCH.COCH.
= 1,5527= 1.5527
n^0 = 1,5549n ^ 0 = 1.5549
= 1,5824= 1.5824
= 1,5454= 1.5454
09 820/120909 820/1209
Auf analoge Weise werden' auch folgende Verbindungen hergestellt: 'The following connections are also established in the same way: '
Verbindung Physikalische DatenConnection physical data
SCNSCN
(sek.) C4H0Sv(sec.) C 4 H 0 Sv
scsrscsr
CH2-CH=CH-ClCH 2 -CH = CH-Cl
(sek.)C4HgS C2H5O(sec) C 4 H g S C 2 H 5 O
CH2-CH=CH-ClCH 2 -CH = CH-Cl
CH2 -C=CH2 Cl = 1,5412CH 2 -C = CH 2 Cl = 1.5412
= 1,5402= 1.5402
=1,5284= 1.5284
20
nD20th
n D
= 1,5313= 1.5313
20
nD20th
n D
= 1,5240= 1.5240
409820/1209409820/1209
75.11.SiS75.11.SiS
Verbindunglink
Physikalische DatenPhysical data
(sek.(sec.
n^0 = 1,5273n ^ 0 = 1.5273
C,C,
CH2-C=CH2 ClCH 2 -C = CH 2 Cl
CHCH
n^0 = 1,5625n ^ 0 = 1.5625
(sek.)C4HgS\ Il(sec.) C 4 H g S \ Il
/SCH3 JH/ SCH 3 JH
n^0 = 1,5605n ^ 0 = 1.5605
A09820/1209A09820 / 1209
A) Insektizide Frässgift,Wirkung A) Insecticidal food poison, effect
Tabakstauden wurden mit einer 0,05%igen wässrigen Wirkstoffemulsion (erhalten aus einem lO%igen emulgierbaren Konzentrat) besprüht.Tobacco bushes were with a 0.05% aqueous active substance emulsion (obtained from a 10% emulsifiable concentrate) sprayed.
Nach dem Antrocknen des Belages wurden die Tabakpflanzen mit Raupen von Spodoptera littoralis im L^-Stadium und von Heliothis virescens im Lo-Stadium besetzt. Der Versuch wurde bei 240C und §0% relativer Luftfeuchtigkeit durchgeführt.After the coating had dried on, the tobacco plants were populated with caterpillars of Spodoptera littoralis in the L ^ stage and of Heliothis virescens in the Lo stage. The experiment was carried out at 24 0 C and §0% relative humidity.
Die Verbindungen gemäss Beispiel 1 zeigten im obigen Test gute Frässgift-Wirkung gegen Spodoptera littoralis und Heliothis virescens. .The compounds according to Example 1 showed in the above test good antifouling action against Spodoptera littoralis and Heliothis virescens. .
B)" Insektizide Kon takt-Wirkung 'B) " Insecticidal contact effect "
Einen Tag vor der Applikation wurden in Töpfen angezogene Puffbohnen (Vicia faba) mit ca. 200 Blattläusen (Aphis fabae) pro Pflanze infiziert. Die Applikation erfolgte mittels Druckluftspritze auf die mit Läusen besetzten Blätter mit einer Spritzbrühe in einer Konzentration von 1000 ppm (hergestellt aus einem 25%igen wettable powder).One day before application, pots were grown Broad beans (Vicia faba) infected with approx. 200 aphids (Aphis fabae) per plant. The application was carried out by means of a compressed air syringe on those with lice covered leaves with a spray mixture in a concentration of 1000 ppm (made from a 25% wettable powder).
Die Bonitierung erfolgte 24 Stunden nach der Applikation. Die Verbindungen gemäss Beispiel 1 zeigten im obigen Test gute Kontakt-Wirkung gegen Aphis-fäbae.The rating took place 24 hours after the application. The compounds according to Example 1 showed in the above test good contact effect against aphis-fäbae.
40982 0/120 940982 0/120 9
Je 6 Reispflanzen der Sorte Caloro wurden in Plastiktöpfen, die einen oberen Durchmesser von 17 cm aufwiesen, verpflanzt und zu einer Höhe von ca. 60 cm aufgezogen. Die Infestation mit Chilo suppressalis Larven (L-, ; 3-4 mm lang) erfolgte 2 Tage nach der Wirkstoffzugabe in Granulatform (Aufwandmenge 8 kg Aktivsubstanz pro Hektare) in das Paddy-Wasser. Die Auswertung auf insektizide Wirkung erfolgte 10 Tage nach der Zugabe des Granulates. Die Verbindungen getnäss Beispiel 1 zeigten im obigen Test gute Wirkung gegen Chilo suppressalis.6 rice plants of the Caloro variety were placed in plastic pots with an upper diameter of 17 cm, transplanted and raised to a height of approx. 60 cm. The infestation with Chilo suppressalis larvae (L-,; 3-4 mm long) took place 2 days after the addition of the active ingredient in Granulate form (application rate 8 kg of active substance per hectare) into the paddy water. The evaluation on insecticidal Effect took place 10 days after the addition of the granules. The compounds according to Example 1 showed good activity against Chilo suppressalis in the above test.
Wirkung gegen Zecken . . Effect against ticks . .
A) Rhipicephalus bursa A) Rhipicephalus bursa
In zwei Versuchsreihen wurden je 5 adulte Zecken bzw. 50 Zeckenlarven in ein Glasröhrchen gezählt und für 1 bis 2 Minuten in 2 ml einer wässrigen Emulsion aus einer VerdUnnungsreihe mit je 100, 10, 1 und 0,1 ppm Testsubstanz getaucht. Das Röhrchen wurde dann mit einem genormten Wattebausch verschlossen und auf den Kopf gestellt, damit die Wirkstoffemulsion von der Watte aufgenommen werden konnte. .In two test series, 5 adult ticks and 50 tick larvae were counted in a glass tube and for 1 to 2 minutes in 2 ml of an aqueous emulsion from a dilution series with 100, 10, 1 and 0.1 ppm each Test substance immersed. The tube was then closed with a standardized cotton ball and turned upside down placed so that the active ingredient emulsion could be absorbed by the cotton wool. .
409820/1209409820/1209
' ""-" "235Ά653'"" - "" 235Ά653
Die Auswertung erfolgte bei den Adulten nach 2 Wochen und bei den Larven nach-2 Tagen. FUr jeden Versuch wurden 2 Wiederholungen durchgeführt.The evaluation of the adults took place after 2 weeks and in the larvae after -2 days. Two repetitions were carried out for each experiment.
Die Verbindungen gemäss Beispiel 1 zeigten im obigen Test gute Wirkung gegen Adulte und Larven von Rhipicephalus bursa. 'The compounds according to Example 1 showed in the above test good effect against adults and larvae of Rhipicephalus bursa. '
B) Boophilus microplus (Larven)B) Boophilus microplus (larvae)
Mit einer analogen VerdUnnungsreihe wie beim Test A wurden mit je 20 OP-sensiblen Larven Versuche durchgeführt. . .,.With an analogous dilution series as in test A, tests were carried out with 20 OP-sensitive larvae each. . .,.
Die Verbindungen gemäss Beispiel 1 zeigten im obigen Test gute Wirkung gegen Larven von Boophilus microplus.The compounds according to Example 1 showed in the above Test good effect against larvae of Boophilus microplus.
■ 409820/1209■ 409820/1209
· 75.11.339· 75.11.339
Phaseolus vulgaris (Buschbohnen) wurden 12 Stunden vor dem Test auf akarizide Wirkung mit einem infestierten BlattstUck aus einer Massenzucht von Tetranychus urticae belegt. Die Übergelaufenen beweglichen Stadien wurden aus einem Chromatographiezerstäuber mit den emulgierten Testpräparaten bestäubt, dass kein Ablaufen der Spritzbrlihe eintrat. Nach zwei bis 7 Tagen wurden Larven, Adulte und Eier unter dem Binokular auf lebende und tote Individuen ausgewertet und das Ergebnis in Prozenten ausgedruckt. Während der "Haltezeit11 standen die behandelten Pflanzen in Gewächshauskabinen bei 25°C.Phaseolus vulgaris (French beans) were coated with an infested piece of leaf from a mass cultivation of Tetranychus urticae 12 hours before the test for acaricidal activity. The moving stages that had overflowed were dusted with the emulsified test preparations from a chromatography atomizer so that the spray mixture did not run off. After two to 7 days, larvae, adults and eggs were evaluated under the binocular for living and dead individuals and the result was printed out as a percentage. During the "holding time 11" , the treated plants stood in greenhouse cabins at 25.degree.
Die Verbindungen gemäss Beispiel 1 zeigten gute Wirkung im obigen Test gegen Eier, Larven und Adulte von Tetranychus urticae. .The compounds according to Example 1 showed a good effect in the above test against eggs, larvae and adults of Tetranychus urticae. .
40982Ö/T20940982Ö / T209
Claims (21)
ILCKII- ■X
ILCKII- ■
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1604372A CH572308A5 (en) | 1972-11-03 | 1972-11-03 | Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides |
CH1363873A CH585018A5 (en) | 1973-09-21 | 1973-09-21 | Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2354653A1 true DE2354653A1 (en) | 1974-05-16 |
Family
ID=25712708
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19732354653 Withdrawn DE2354653A1 (en) | 1972-11-03 | 1973-10-31 | NEW ESTERS |
Country Status (11)
Country | Link |
---|---|
US (2) | US3898305A (en) |
JP (1) | JPS4975732A (en) |
AT (1) | AT324772B (en) |
CA (1) | CA1058192A (en) |
DE (1) | DE2354653A1 (en) |
EG (1) | EG11386A (en) |
FR (1) | FR2205526B1 (en) |
GB (1) | GB1441639A (en) |
IL (1) | IL43458A (en) |
NL (1) | NL7314564A (en) |
OA (1) | OA04500A (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4017612A (en) * | 1972-11-03 | 1977-04-12 | Ciba-Geigy Corporation | Combatting insects and acarids with certain O-methyl/ethyl-S-propyl/butyl-O-phenyl-thiophosphates and -dithiophosphates |
CA1058192A (en) * | 1972-11-03 | 1979-07-10 | Ciba-Geigy Ag | Esters |
US4029774A (en) * | 1974-06-26 | 1977-06-14 | Rohm And Haas Company | O,S-dialkyl O -phenylthio-phenyl phosphorothiolates/phosphorodithioates and their derivatives and pesticidal use |
US4086337A (en) * | 1976-06-16 | 1978-04-25 | Rohm And Haas Company | O,S-dialkyl O(S)-sulfonyloxy(thio)phenyl phosphorothiolates and phosphorodi(tri)thioates |
CA1052688A (en) * | 1975-11-18 | 1979-04-17 | American Cyanamid Company | Liquid compositions containing a polyethylene glycol safener and an organophosphorus pesticide |
US4436736A (en) | 1982-03-29 | 1984-03-13 | Union Carbide Corporation | Methods for controlling pests with substituted phenyl thio(thiono)phosphates and the thio(thiono)phosphates |
DE3223949A1 (en) * | 1982-06-26 | 1983-12-29 | Celamerck Gmbh & Co Kg, 6507 Ingelheim | THIOLPHOSPHORIC ACID ESTERS, THEIR PRODUCTION AND USE |
DE3239288A1 (en) * | 1982-10-23 | 1984-04-26 | Basf Ag, 6700 Ludwigshafen | DIHALOGENVINYLPHENYL-PHOSPHORIC ACID ESTER, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PEST CONTROL |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3087855A (en) * | 1959-01-23 | 1963-04-30 | Coull James | Omicron-higher alkenylphenyl omicron, omicron-dialkyl thionophosphate triester compou |
BE633592A (en) * | 1962-06-15 | |||
US3317561A (en) * | 1963-05-29 | 1967-05-02 | American Cyanamid Co | New heterocyclic organo-phosphate compounds |
JPS4924656B1 (en) * | 1970-03-13 | 1974-06-25 | ||
CA1058192A (en) * | 1972-11-03 | 1979-07-10 | Ciba-Geigy Ag | Esters |
-
1973
- 1973-10-16 CA CA183,449A patent/CA1058192A/en not_active Expired
- 1973-10-22 IL IL43458A patent/IL43458A/en unknown
- 1973-10-23 US US408874A patent/US3898305A/en not_active Expired - Lifetime
- 1973-10-23 NL NL7314564A patent/NL7314564A/xx not_active Application Discontinuation
- 1973-10-30 OA OA55050A patent/OA04500A/en unknown
- 1973-10-31 FR FR7338840A patent/FR2205526B1/fr not_active Expired
- 1973-10-31 DE DE19732354653 patent/DE2354653A1/en not_active Withdrawn
- 1973-11-01 EG EG414/73A patent/EG11386A/en active
- 1973-11-02 GB GB5107073A patent/GB1441639A/en not_active Expired
- 1973-11-02 JP JP48123910A patent/JPS4975732A/ja active Pending
- 1973-11-02 AT AT924773A patent/AT324772B/en not_active IP Right Cessation
-
1976
- 1976-12-17 US US05/751,918 patent/US4262012A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US3898305A (en) | 1975-08-05 |
IL43458A (en) | 1976-11-30 |
NL7314564A (en) | 1974-05-07 |
AU6170573A (en) | 1975-04-24 |
AT324772B (en) | 1975-09-25 |
GB1441639A (en) | 1976-07-07 |
FR2205526B1 (en) | 1978-11-17 |
EG11386A (en) | 1977-04-30 |
FR2205526A1 (en) | 1974-05-31 |
OA04500A (en) | 1980-03-30 |
US4262012A (en) | 1981-04-14 |
JPS4975732A (en) | 1974-07-22 |
IL43458A0 (en) | 1974-01-14 |
CA1058192A (en) | 1979-07-10 |
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